Bloch
Bloch-Sulzberger Syndrome
Bloch-Sulzberger Syndrome (pronounced: blohk-suhlz-bur-ger sin-drohm), also known as Incontinentia Pigmenti, is a rare genetic disorder that primarily affects the skin, eyes, and central nervous system.
Etymology
The syndrome is named after the Swiss dermatologist Bruno Bloch and the American dermatologist Marion Baldur Sulzberger who first described the condition in 1928.
Definition
Bloch-Sulzberger Syndrome is a condition that affects the development of several parts of the body. The most noticeable characteristic is a skin abnormality that evolves throughout childhood and adolescence. Other potential complications include dental abnormalities, eye problems that can lead to vision loss, and, in some cases, neurological issues.
Symptoms
The symptoms of Bloch-Sulzberger Syndrome can vary greatly from person to person. They may include:
- Skin Lesions: These often follow a pattern known as the "Lines of Blaschko" and can evolve over time.
- Dental Abnormalities: These can include missing or peg-shaped teeth.
- Eye Abnormalities: These can include retinal detachment or cataracts, which can lead to vision loss.
- Neurological Abnormalities: These can include seizures, intellectual disability, and motor delays.
Treatment
There is currently no cure for Bloch-Sulzberger Syndrome. Treatment is symptomatic and supportive, often involving a team of specialists. Dermatologists, ophthalmologists, neurologists, and dentists may all be involved in the care of a person with this condition.
See Also
External links
- Medical encyclopedia article on Bloch
- Wikipedia's article - Bloch
This WikiMD article is a stub. You can help make it a full article.
Languages: - East Asian
中文,
日本,
한국어,
South Asian
हिन्दी,
Urdu,
বাংলা,
తెలుగు,
தமிழ்,
ಕನ್ನಡ,
Southeast Asian
Indonesian,
Vietnamese,
Thai,
မြန်မာဘာသာ,
European
español,
Deutsch,
français,
русский,
português do Brasil,
Italian,
polski